Juneja Saurabh, Katyal Sonal, Rathore Ajit Singh, Shetty Devi Charan, Tandon Ankita, Jain Pankaj
Department of Oral Pathology, I.T.S-CDSR, Ghaziabad, Uttar Pradesh, India.
J Cytol. 2019 Apr-Jun;36(2):111-115. doi: 10.4103/JOC.JOC_230_16.
The term oral potentially malignant disorder (OPMD) was recommended to refer to precancer as it conveys that not all disorders described under this term may transform into cancer. Oral squamous cell carcinoma (OSCC) arises through an accumulation of genetic alterations, deoxy ribonucleic acid (DNA) changes, and epigenetic alterations. Thus, a simple yet a sensitive and specific test for early diagnosis is the need of an hour. The micronuclei (MN) assay in exfoliated epithelial cells is potentially an excellent biomarker to detect chromosome loss or malfunction of mitotic spindle.
To compare the frequency of MN in exfoliated cells from oral mucosa exposed to genotoxic agents using different staining procedures and to observe the incidence of micronucleus in potentially malignant and malignant lesions.
The study was undertaken to observe the cytogenetic damage in the exfoliated buccal cells of 75 cases of tobacco-related PMDs, OSCC and control subjects (25 cases from each group) and were evaluated with nonspecific May-Grünwald Giemsa stain and DNA-specific Feulgen stain. The results were statistically determined using SPSS version 17.0.
Correlation analyses in the present study depicted that MN frequency was significantly more in oral squamous cell carcinoma than OPMDs and normal group ( < 0.05). Giemsa-stained slides correlated significantly with karyorrhexis, karyolysis, condensed chromatin, and binucleates, whereas no such correlations were found with DNA-specific stains.
Malignant transformation is accompanied by loss of cell capacity to evolve to death in situations of DNA damage. These findings indicate that nuclear anomalies may be misinterpreted as MN with nonspecific DNA stains and lead to false-positive results in studies with cells of epithelial origin.
口腔潜在恶性疾病(OPMD)这一术语被推荐用于指代癌前病变,因为它表明并非该术语下描述的所有疾病都会转变为癌症。口腔鳞状细胞癌(OSCC)是通过基因改变、脱氧核糖核酸(DNA)变化和表观遗传改变的积累而发生的。因此,当下急需一种简单且灵敏特异的早期诊断检测方法。脱落上皮细胞中的微核(MN)检测有可能成为检测染色体丢失或有丝分裂纺锤体功能异常的极佳生物标志物。
使用不同染色程序比较暴露于基因毒性剂的口腔黏膜脱落细胞中微核的频率,并观察潜在恶性和恶性病变中微核的发生率。
本研究旨在观察75例烟草相关口腔潜在恶性疾病、口腔鳞状细胞癌患者及对照受试者(每组25例)颊部脱落细胞的细胞遗传学损伤,并用非特异性的美蓝-吉姆萨染色和DNA特异性的福尔根染色进行评估。结果使用SPSS 17.0版进行统计学分析。
本研究的相关性分析表明,口腔鳞状细胞癌中的微核频率显著高于口腔潜在恶性疾病组和正常组(<0.05)。吉姆萨染色的玻片与核碎裂、核溶解、染色质浓缩和双核显著相关,而DNA特异性染色未发现此类相关性。
恶性转化伴随着细胞在DNA损伤情况下向死亡进化能力的丧失。这些发现表明,在起源于上皮的细胞研究中,核异常可能会被非特异性DNA染色误判为微核,从而导致假阳性结果。